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Nucleic acid amplification techniques (NAATs) are the gold standard methods for the identification of specific genomic sequences. NAATs, including polymerase chain reaction (PCR), ligase chain reaction, transcription mediated amplification, nucleic acid sequence-based amplification, are highly specific and sensitive to both RNA and DNA templates. Isothermal amplification techniques have become particularly important in the development of rapid and cost-effective diagnostics, since they require only a single temperature.
Emulsion PCR represents a particularly simple means for combining sample miniaturization with compartmentalization. Formation of >106 individual W/O colliodal emulsion droplets promotes isolation of single target templates, thus decreasing the likelihood of non-specific amplification, while improving assay accuracy and its limit-of-detection.